全文获取类型
收费全文 | 256篇 |
免费 | 9篇 |
专业分类
化学 | 233篇 |
力学 | 1篇 |
数学 | 9篇 |
物理学 | 22篇 |
出版年
2017年 | 1篇 |
2016年 | 7篇 |
2015年 | 2篇 |
2014年 | 8篇 |
2013年 | 4篇 |
2012年 | 13篇 |
2011年 | 20篇 |
2010年 | 11篇 |
2009年 | 13篇 |
2008年 | 21篇 |
2007年 | 15篇 |
2006年 | 32篇 |
2005年 | 27篇 |
2004年 | 16篇 |
2003年 | 9篇 |
2002年 | 8篇 |
2001年 | 3篇 |
2000年 | 5篇 |
1999年 | 4篇 |
1998年 | 3篇 |
1996年 | 3篇 |
1991年 | 3篇 |
1990年 | 1篇 |
1989年 | 3篇 |
1988年 | 5篇 |
1987年 | 4篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1982年 | 1篇 |
1981年 | 2篇 |
1980年 | 2篇 |
1979年 | 1篇 |
1978年 | 1篇 |
1974年 | 1篇 |
1965年 | 2篇 |
1964年 | 2篇 |
1963年 | 2篇 |
1962年 | 1篇 |
1961年 | 1篇 |
1955年 | 1篇 |
1954年 | 1篇 |
1943年 | 1篇 |
1924年 | 1篇 |
1923年 | 1篇 |
1909年 | 1篇 |
排序方式: 共有265条查询结果,搜索用时 187 毫秒
251.
Li H Hollamby MJ Seki T Yagai S Möhwald H Nakanishi T 《Langmuir : the ACS journal of surfaces and colloids》2011,27(12):7493-7501
An N-methylfulleropyrrolidine (2) bearing three eicosyloxy chains on the laterally substituted phenyl group can be further functionalized to give the ionic fullerene derivative, i.e., N,N-dimethylfulleropyrrolidinium iodide (1). The spectroscopic, electrochemical, self-assembly, and liquid crystalline properties of 1 have been investigated and compared to its neutral precursor 2. Changes in electronic structure upon ionization are observed in the UV spectra. Additionally, a positive potential shift of electrochemical reductions for 1 compared to those of 2 is noted in both homogeneous solution and film state. Driven by the π-π, van der Waals, and electrostatic interactions, the ionic compound 1 is able to form a variety of functional and polymorphic self-assembled structures both from solution and on substrates, including hierarchically organized flakelike microparticles with high water repellency, doughnut-shaped objects with rough surfaces, and long one-dimensional C(60) nanowires (>1 μm). The thermotropic behavior of 1 has also been investigated, and a smectic liquid crystalline phase was observed at elevated temperatures. Further investigations of the thermotropic behavior of 1 revealed that a deionization back-reaction from 1 to the neutral precursor 2 gradually occurred. The mechanism of this deionization reaction is presented and discussed. These investigations provide insight into the effects of added ionicity to alkylated fullerene derivatives, in particular on their self-assembly features and functionality. 相似文献
252.
Stefaniu C Chanana M Wang D Novikov DV Brezesinski G Möhwald H 《Langmuir : the ACS journal of surfaces and colloids》2011,27(3):1192-1199
The interfacial properties of Fe(3)O(4)@MEO(2)MA(90)-co-OEGMA(10) NPs, recently developed and described as promising nanotools for biomedical applications, have been investigated at the air/water interface. These Fe(3)O(4) NPs, capped with catechol-terminated random copolymer brushes of 2-(2-methoxyethoxy) ethyl methacrylate (MEO(2)MA) and oligo(ethylene glycol) methacrylate (OEGMA), with molar fractions of 90% and 10%, respectively, proved to be surface active. Surface tension measurements of aqueous dispersions of the NPs showed that the adsorption of the NPs at the air/water interface is time- and concentration-dependent. These NPs do not behave as classical amphiphiles. Once adsorbed at the air/water interface, they do not exchange with NPs in bulk, but they are trapped at the interface. This means that all NPs from the bulk adsorb to the interface until reaching maximum coverage of the interface, which corresponds to values between 6 × 10(-4) and 8 × 10(-4) mg/cm(2) and a critical equilibrium surface tension of ~47 mN/m. Moreover, Langmuir layers of Fe(3)O(4)@MEO(2)MA(90)-co-OEGMA(10) NPs have been investigated by measuring surface pressure-area compression-expansion isotherms and in situ X-ray fluorescence spectra. The compression-expansion isotherms showed a plateau region above a critical surface pressure of ~25 mN/m and a pronounced hysteresis. By using a special one-barrier Langmuir trough equipped with two surface pressure microbalances, we have shown that the NPs are squeezed out from the interface into the aqueous subphase, and they readsorb on the other side of the barrier. The results have been supported by TEM as well as AFM experiments of transferred Langmuir-Schaefer films on solid supports. This study shows the ability of Fe(3)O(4)@MEO(2)MA(90)-co-OEGMA(10) NPs to transfer from hydrophilic media (an aqueous solution) to the hydrophobic/hydrophilic interface (air/water interface) and back to the hydrophilic media. This behavior is very promising, opening studies of their ability to cross biological membranes. 相似文献
253.
Radziuk D Skirtach A Gessner A Kumke MU Zhang W Möhwald H Shchukin D 《Langmuir : the ACS journal of surfaces and colloids》2011,27(23):14472-14480
Ultrasound (20 kHz, 29 W·cm(-2)) is employed to form three types of erbium oxide nanoparticles in the presence of multiwalled carbon nanotubes as a template material in water. The nanoparticles are (i) erbium carboxioxide nanoparticles deposited on the external walls of multiwalled carbon nanotubes and Er(2)O(3) in the bulk with (ii) hexagonal and (iii) spherical geometries. Each type of ultrasonically formed nanoparticle reveals Er(3+) photoluminescence from crystal lattice. The main advantage of the erbium carboxioxide nanoparticles on the carbon nanotubes is the electromagnetic emission in the visible region, which is new and not examined up to the present date. On the other hand, the photoluminescence of hexagonal erbium oxide nanoparticles is long-lived (μs) and enables the higher energy transition ((4)S(3/2)-(4)I(15/2)), which is not observed for spherical nanoparticles. Our work is unique because it combines for the first time spectroscopy of Er(3+) electronic transitions in the host crystal lattices of nanoparticles with the geometry established by ultrasound in aqueous solution of carbon nanotubes employed as a template material. The work can be of great interest for "green" chemistry synthesis of photoluminescent nanoparticles in water. 相似文献
254.
Zhang D Kremer RK Lemmens P Choi KY Liu J Whangbo MH Berger H Skourski Y Johnsson M 《Inorganic chemistry》2011,50(24):12877-12885
Two new isostructural layered oxohalides FeTe(3)O(7)X (X = Cl, Br) were synthesized by chemical vapor transport reactions, and their crystal structures and magnetic properties were characterized by single-crystal X-ray diffraction, Raman spectroscopy, magnetic susceptibility and magnetization measurements, and also by density functional theory (DFT) calculations of the electronic structure and the spin exchange parameters. FeTe(3)O(7)X crystallizes in the monoclinic space group P2(1)/c with the unit cell parameters a = 10.7938(5), b = 7.3586(4), c = 10.8714(6) ?, β = 111.041(5)°, Z = 4 for FeTe(3)O(7)Cl, and a = 11.0339(10), b = 7.3643(10), c = 10.8892(10) ?, β = 109.598(10)°, Z = 4 for FeTe(3)O(7)Br. Each compound has one unique Fe(3+) ion coordinating a distorted [FeO(5)] trigonal bipyramid. Two such groups share edges to form [Fe(2)O(8)] dimers that are isolated from each other by Te(4+) ions. The high-temperature magnetic properties of the compounds as well as spectroscopic investigations are consistent with an isolated antiferromagnetic spin dimer model with almost similar spin gaps of ~35 K for X = Cl and Br, respectively. However, deviations at low temperatures in the magnetic susceptibility and the magnetization data indicate that the dimers couple via an interdimer coupling. This interpretation is also supported by DFT calculations which indicate an interdimer exchange which amounts to 25% and 10% of the intradimer exchange for X = Cl and Br, respectively. The magnetic properties support the counterion character and a weak integration of halide ions into the covalent network similar to that in many other oxohalides. 相似文献
255.
Teng XR Shchukin DG Möhwald H 《Langmuir : the ACS journal of surfaces and colloids》2008,24(2):383-389
A novel lipophilic drug carrier, "oil-in-water" multifunctional composite nanocontainers, is developed by combining ultrasonic technique and layer-by-layer assembly. Polyglutamate/polyethyleneimine/poly(acrylic acid) nanocontainers loaded with the lipophilic drug, rifampicin, dissolved in soybean oil were fabricated. Raman confocal microscopy and scanning electron microscopy proved the successful incorporation of rifampicin into composite water-dispersible polyglutamate/polyelectrolyte nanocontainers. Transmission electron microscopy and confocal laser scanning microscopy indicated that the drug can be released by changing the pH value of the media due to the pH-responsive properties of the polyglutamate/polyelectrolyte shell. 相似文献
256.
He Q Song W Möhwald H Li J 《Langmuir : the ACS journal of surfaces and colloids》2008,24(10):5508-5513
The assembled polyelectrolyte nanotubes composed of poly(styrenesulfonate) and poly(allylamine hydrochloride) multilayers by using the layer-by-layer assembly combined with the porous template method can be transformed into capsules by a high-temperature treatment. Scanning electron microscopy and confocal laser scanning microscopy images revealed the whole transition process. The structure transformation of polyelectrolyte multilayers after annealing can be initiated by the input of thermal energy which leads to a breakage of ion pairs between oppositely charged polyelectrolyte groups. The transition process from tubes to capsules is supposed to be driven by the Raleigh instability and leads to the generated polyelectrolyte capsules with different sizes. 相似文献
257.
Santhosh Babu S Aimi J Ozawa H Shirahata N Saeki A Seki S Ajayaghosh A Möhwald H Nakanishi T 《Angewandte Chemie (International ed. in English)》2012,51(14):3391-3395
Illuminating! Isolation of a π-core by covalently attached flexible hydrocarbon chains has been employed to synthesize blue-emitting oligo(p-phenylenevinylene) (OPV) liquids with tunable viscosity and optical properties. A solvent-free, stable, white-light emitting ink/paint, which can be applied onto various surfaces and even onto LEDs, was made by blending of liquid OPVs with emissive solid dopants. 相似文献
258.
Liu S Möhwald H Volkmer D Kurth DG 《Langmuir : the ACS journal of surfaces and colloids》2006,22(5):1949-1951
Molecular or supramolecular systems capable of electro- and photostimulated color changes are still rare. We present a device design based on an electrostatic complex of a nanoscopic polyoxometalate cluster and a polyelectrolyte. The coating reversibly changes color from transparent to blue by photo- and/or electroinduced stimulation. The choice of the components results in perfect transparency over the entire visible range, a large optical response, reversible operation, and excellent stability. 相似文献
259.
This work demonstrates the potential of sonochemistry to become a most valuable tool for nanotechnology if the underlying complex processes are understood and controlled. It is shown that control of cavitation requires controlling of interfaces at the microsec time scale and thus a diversity of phenomena are observed using different surfactants. By means of concrete examples it is shown that non-equilibrium nanostructures, e.g. Ru/Pt core-shell nanoparticles can be prepared. Hollow microbubbles with nanoparticles in the wall, which may contain gases over weeks, can be constructed by sonication of the corresponding colloid solutions. 相似文献
260.